Valerie Dubois

Valerie is a quality and regulatory professional with extensive experience in neuromodulation, cardiovascular, and endovascular applications. She has successfully taken medical devices from research and prototype stages through to human use and regulatory approval (IDE, PMA, de novo, CE Marking). Leveraging her expertise in global compliance, clinical operations, and product development, Valerie ensures that products are safe, effective, and market ready. From concept to commercialization, she guides teams through regulations and standards while fostering innovation and continuous improvement, with the ultimate goal of advancing new standards of care. Valerie holds a Master's degree in Biomechanics.